ClinVar Miner

List of variants in gene LHB studied for Leydig cell hypoplasia

Included ClinVar conditions (4):
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Gene type:
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Total variants: 10
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HGVS dbSNP
NM_000894.2(LHB):c.114C>G (p.Val38=) rs6521
NM_000894.2(LHB):c.132A>C (p.Pro44=) rs1056914
NM_000894.2(LHB):c.16-26T>C rs4002462
NM_000894.2(LHB):c.167G>A (p.Gly56Asp) rs121912517
NM_000894.2(LHB):c.183+11T>C rs2387588
NM_000894.2(LHB):c.183+1G>C rs786204822
NM_000894.2(LHB):c.183+1G>T rs786204822
NM_000894.2(LHB):c.221A>G (p.Gln74Arg) rs5030773
NM_000894.2(LHB):c.28_39del (p.Leu10_Leu13del) rs769066903
NM_000894.2(LHB):c.88_96del (p.His30_Ile32del) rs786204823

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